GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease

نویسندگان

  • Carlos Cruchaga
  • John S.K. Kauwe
  • Oscar Harari
  • Sheng Chih Jin
  • Yefei Cai
  • Celeste M. Karch
  • Bruno A. Benitez
  • Amanda T. Jeng
  • Tara Skorupa
  • David Carrell
  • Sarah Bertelsen
  • Matthew Bailey
  • David McKean
  • Joshua M. Shulman
  • Philip L. De Jager
  • Lori Chibnik
  • David A. Bennett
  • Steve E. Arnold
  • Denise Harold
  • Rebecca Sims
  • Amy Gerrish
  • Julie Williams
  • Vivianna M. Van Deerlin
  • Virginia M.-Y. Lee
  • Leslie M. Shaw
  • John Q. Trojanowski
  • Jonathan L. Haines
  • Richard Mayeux
  • Margaret A. Pericak-Vance
  • Lindsay A. Farrer
  • Gerard D. Schellenberg
  • Elaine R. Peskind
  • Douglas Galasko
  • Anne M. Fagan
  • David M. Holtzman
  • John C. Morris
  • Alison M. Goate
چکیده

Cerebrospinal fluid (CSF) tau, tau phosphorylated at threonine 181 (ptau), and Aβ₄₂ are established biomarkers for Alzheimer's disease (AD) and have been used as quantitative traits for genetic analyses. We performed the largest genome-wide association study for cerebrospinal fluid (CSF) tau/ptau levels published to date (n = 1,269), identifying three genome-wide significant loci for CSF tau and ptau: rs9877502 (p = 4.89 × 10⁻⁹ for tau) located at 3q28 between GEMC1 and OSTN, rs514716 (p = 1.07 × 10⁻⁸ and p = 3.22 × 10⁻⁹ for tau and ptau, respectively), located at 9p24.2 within GLIS3 and rs6922617 (p = 3.58 × 10⁻⁸ for CSF ptau) at 6p21.1 within the TREM gene cluster, a region recently reported to harbor rare variants that increase AD risk. In independent data sets, rs9877502 showed a strong association with risk for AD, tangle pathology, and global cognitive decline (p = 2.67 × 10⁻⁴, 0.039, 4.86 × 10⁻⁵, respectively) illustrating how this endophenotype-based approach can be used to identify new AD risk loci.

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عنوان ژورنال:
  • Neuron

دوره 78  شماره 

صفحات  -

تاریخ انتشار 2013